alprazolam

Generic: alprazolam

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name alprazolam
Generic Name alprazolam
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

alprazolam 1 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-614
Product ID 71205-614_0221ed96-545d-7ceb-e063-6394a90a528a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA018276
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 1981-10-16

Pharmacologic Class

Established (EPC)
benzodiazepine [epc]
Chemical Structure
benzodiazepines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205614
Hyphenated Format 71205-614

Supplemental Identifiers

RxCUI
197321
UPC
0371205614300
UNII
YU55MQ3IZY
NUI
N0000175694 M0002356

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name alprazolam (source: ndc)
Generic Name alprazolam (source: ndc)
Application Number NDA018276 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 2 TABLET in 1 BOTTLE (71205-614-02)
  • 30 TABLET in 1 BOTTLE (71205-614-30)
  • 60 TABLET in 1 BOTTLE (71205-614-60)
  • 90 TABLET in 1 BOTTLE (71205-614-90)
source: ndc

Packages (4)

71205-614-02 2 TABLET in 1 BOTTLE (71205-614-02) 71205-614-30 30 TABLET in 1 BOTTLE (71205-614-30) 71205-614-60 60 TABLET in 1 BOTTLE (71205-614-60) 71205-614-90 90 TABLET in 1 BOTTLE (71205-614-90)

Ingredients (1)

alprazolam (1 mg/1)

Linked Drug Pages (1)

Alprazolam ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0221ed96-545d-7ceb-e063-6394a90a528a", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0371205614300"], "unii": ["YU55MQ3IZY"], "rxcui": ["197321"], "spl_set_id": ["10de2b3b-3b3f-4a5a-a9e7-a8401f53b8cc"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET in 1 BOTTLE (71205-614-02)", "package_ndc": "71205-614-02", "marketing_start_date": "20211015"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-614-30)", "package_ndc": "71205-614-30", "marketing_start_date": "20211015"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-614-60)", "package_ndc": "71205-614-60", "marketing_start_date": "20211015"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-614-90)", "package_ndc": "71205-614-90", "marketing_start_date": "20211015"}], "brand_name": "Alprazolam", "product_id": "71205-614_0221ed96-545d-7ceb-e063-6394a90a528a", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "71205-614", "dea_schedule": "CIV", "generic_name": "alprazolam", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": "1 mg/1"}], "application_number": "NDA018276", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "19811016", "listing_expiration_date": "20261231"}